恐溶剂的
弹性体
锂(药物)
材料科学
金属锂
保形涂层
电解质
涂层
电化学
金属
聚碳酸酯
单体
离子电导率
聚合物
化学工程
钝化
离子键合
阴极
纳米技术
离子液体
光致聚合物
电化学窗口
渗透(战争)
表面改性
粘附
纳米复合材料
碳酸丙烯酯
储能
制作
作者
Seung Ho Kwon,Hyeonjae Jo,Junghun Han,Young Ham,Taek-Soo Kim,Michael J. Lee,Han-Hee Cho,Jinseok Park,Yun‐Hi Kim
标识
DOI:10.1021/acsenergylett.5c04250
摘要
The interfacial instability and dendritic growth of lithium (Li) remain key obstacles to the implementation of Li metal batteries (LMBs). Herein, we present in situ-formed polymer protective layers (PPLs) on Li to enhance interfacial stability and electrochemical performance. The PPLs comprise a fluorinated elastomer and Li6.4La3Zr1.4Ta0.6O12 fillers to tune mechanical integrity and ionic conductivity. While in situ photopolymerization enables conformal coating on Li, the fluorinated monomers are tailored to optimize solvophobicity for carbonate electrolytes. Among them, hexafluorobutyl acrylate-based PPL (H-PPL) exhibits optimal solvophobicity with an ionic conductivity of 0.20 mS cm–1, stretchability of 300%, and an adhesion strength of 5.1 N m–1, which suppresses electrolyte penetration and promotes uniform Li deposition. Consequently, full cells employing H-PPL-coated Li and LiNi0.8Co0.1Mn0.1O2 cathodes retain 87.8% capacity after 250 cycles at 1C, outperforming bare Li (67.6%). This study demonstrates that PPL with controlled solvophobicity leads to improved electrochemical performance of LMBs.
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